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HRID 561467作成日:2026年10月27日

4-Chloro-alpha-cyclopropyl-alpha-methylbenzenemethanol → 1-(Benzo[d][1,3]dioxol-5-yl)-1-cyclopropylethanol

https://huagongshe.com/reaction/561467

反応式

関与物質

役割名称HCID仕込み量
反応物4-Chloro-alpha-cyclopropyl-alpha-methylbenzenemethanolHCID 23463—
反応物AcetopiperoneHCID 76622—
反応物HCID 178418630HCID 178418630—
溶媒TetrahydrofuranHCID 8028—
生成物1-(Benzo[d][1,3]dioxol-5-yl)-1-cyclopropylethanolHCID 58392261—

反応手順

The title compound was prepared starting from 1.50 g (9.14 mmol) of 3,4-(methylenedioxy)acetophenone and 36.5 ml (18.28 mmol) of a 0.5N solution of cyclopropylmagnesium bromide in tetrahydrofuran in analogy to the synthesis of the compound from Example 138A. 1.32 g (70% of theory) of the title compound were obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063234B2
出典データセットuspto-grants-2011_11
ORD IDord-83377f42d1354a9da6ac332978b01b77
出典メモuspto-grants-2011_11